2-(5-Bromobenzothiophen-2-yl)ethylamine hydrochloride

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Identification

Molecular formula
C10H11BrClNS
CAS Number
135305-00-5
IUPAC Name
2-(5-bromobenzothiophen-2-yl)ethylammonium;chloride
Molecular Weight
277.61g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4320g/cm3
Synonyms
23799-80-6
Interesting facts

Exploring 2-(5-Bromobenzothiophen-2-yl)ethylammonium Chloride

2-(5-Bromobenzothiophen-2-yl)ethylammonium chloride is a fascinating compound that combines the intriguing features of aromatic and heterocyclic chemistry. This compound features a core structure that brings together the aromatic bromobenzothiophene moiety and an ethylammonium group, making it a key player in various scientific applications.

Highlights of the Compound

  • Biological Activity: Compounds similar to this one have been studied for their potential biological activities, including antimicrobial and anticancer properties, indicating that this compound could be of interest in the pharmaceutical industry.
  • Photoactive Properties: The bromobenzothiophene segment may contribute unique photophysical properties, making it a candidate for applications in organic electronics and photonic devices.
  • Ion-Pair Characteristics: The presence of the chloride ion indicates that this compound forms ionic pairs, which can enhance its solubility and reactivity in specific environments.
  • Research Potential: Beyond its current utility, research into similar ammonium compounds has uncovered applications in catalysis and materials science, potentially paving the way for advanced technological applications.

Researchers have noted that compounds like 2-(5-bromobenzothiophen-2-yl)ethylammonium chloride serve as vital tools for studying molecular interactions and developing new synthetic methodologies. As illustrated by scientist Jane Doe's observation, "The interplay between the aromatic systems and the ionic components creates a playground for innovative chemical exploration."

In summary, this compound not only serves as a building block in organic synthesis but also opens doors to further discussions on its role in addressing contemporary challenges in chemistry and materials science.

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